Waack Ursula, Nicholson Tracy L
United States Department of Energy, Oak Ridge Institute for Science and Education, Oak Ridge, TN, United States.
United States Department of Agriculture, National Animal Disease Center, Agricultural Research Service, Ames, IA, United States.
Front Microbiol. 2018 Nov 6;9:2707. doi: 10.3389/fmicb.2018.02707. eCollection 2018.
is a bacterial swine pathogen with a significant economic burden. It typically colonizes the tonsil and nasal cavity of swine causing a variety of symptoms ranging from asymptomatic carriage to lethal systemic disease. A key barrier toward the development of improved vaccines or interventions for infections is a gap in our understanding of the mechanisms contributing to persistence in the host, in which colonized pigs continue to shed and transmit We hypothesized that exposure to sub-MICs of antibiotics commonly used by the swine industry would increase the biofilm capacity of strains. Using a 96-well plate MIC protocol, we experimentally determined the MIC for each of 12 antibiotics for a virulent strain of strain that consistently formed biofilms using a standard crystal violet assay. Using this static biofilm assay, we demonstrated that sub-MICs of bacitracin, carbadox, chlortetracycline, enrofloxacin, gentamicin, neomycin, sulfadimethoxine, tiamulin, and tylosin did not increase biofilms. In contrast, we demonstrated that sub-MICs of amoxicillin, lincomycin, and oxytetracycline increased overall biofilm formation under both static and flow conditions. The biofilm formation of 11 additional clinical isolates were measured using the relevant concentrations of amoxicillin, lincomycin, and oxytetracycline. Eight of the eleven strains increased the biofilm formation with lincomycin, seven with amoxicillin, and three with oxytetracycline. Collectively, our data demonstrate that exposure to sub-MICs of these commonly used antibiotics contributes to increased biofilm formation of , thereby potentially increasing survival and persistence within the respiratory tract of swine.
是一种给养猪业带来巨大经济负担的猪源细菌性病原体。它通常定植于猪的扁桃体和鼻腔,可引发从无症状携带到致死性全身疾病等多种症状。开发针对该感染的改良疫苗或干预措施的一个关键障碍是,我们对其在宿主体内持续存在机制的理解存在差距,在这种情况下,定植的猪会持续排出并传播该病原体。我们假设,接触养猪业常用抗生素的亚抑菌浓度会增加该菌株的生物膜形成能力。使用96孔板微量肉汤稀释法,我们通过标准结晶紫测定法实验确定了12种抗生素对一株持续形成生物膜的强毒株的最低抑菌浓度(MIC)。使用这种静态生物膜测定法,我们证明杆菌肽、卡巴氧、金霉素、恩诺沙星、庆大霉素、新霉素、磺胺二甲氧嘧啶、泰妙菌素和泰乐菌素的亚抑菌浓度不会增加该菌株的生物膜形成。相比之下,我们证明阿莫西林、林可霉素和土霉素的亚抑菌浓度在静态和流动条件下均会增加总体生物膜形成。使用阿莫西林、林可霉素和土霉素的相关浓度测定了另外11株临床分离株的生物膜形成情况。11株菌株中有8株使用林可霉素后生物膜形成增加,7株使用阿莫西林后增加,3株使用土霉素后增加。总体而言,我们的数据表明,接触这些常用抗生素的亚抑菌浓度会导致该菌株生物膜形成增加,从而可能增加其在猪呼吸道内的存活和持续存在能力。